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1.
J Med Entomol ; 57(4): 1239-1245, 2020 07 04.
Artigo em Inglês | MEDLINE | ID: mdl-32112094

RESUMO

Aedes aegypti (L.) (Diptera: Culicidae) is a diurnal feeder that lives in close association with human populations. It is the principal vector of yellow fever, dengue fever and the Zika Virus. Issues of arboviral diseases have been on the ascendency in most countries including Ghana where Aedes mosquito is the main vector of yellow fever. A comparative study of the biting behavior of Ae. aegypti and the identification of subspecies were undertaken using molecular technique. Standard human landing technique was used to collect both indoor and outdoor biting mosquitoes at three zones located in the Upper East (Bolgatanga), Upper West (Nadowli), and Northern (Damongo) Regions of Ghana during the dry and rainy seasons between 0600 and 1800 Greenwich Mean Time (GMT). All collected mosquitoes were identified morphologically using taxonomic keys. random amplified polymorphic DNA polymerase chain reaction was used to categorize Ae. aegypti into subspecies. Adult female Aedes mosquitoes identified formed 62% (n = 1,206) of all female mosquitoes collected. Aedes aegypti 98% and Aedes vittatus 2% were the only Aedes species identified. Bolgatanga recorded the largest number of Ae. aegypti 42%, whereas Nadowli 22% recorded the least. Aedes vittatus was observed in Nadowli. Aedes aegypti exhibited a bimodal biting behavior peaking at 0600-0800 GMT and 1500-1600 h GMT. Molecular findings revealed 69% Ae. aegypti aegypti and 31% Ae. aegypti formosus as the two subspecies (n = 110). This information is important for implementing effective vector control programs in the three regions of the northern Ghana.


Assuntos
Aedes/fisiologia , Mosquitos Vetores/fisiologia , Aedes/anatomia & histologia , Aedes/genética , Distribuição Animal , Animais , Gana , Mordeduras e Picadas de Insetos , Proteínas de Insetos/análise , Mosquitos Vetores/anatomia & histologia , Mosquitos Vetores/genética , Febre Amarela/transmissão
2.
PLoS Negl Trop Dis ; 13(8): e0007115, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-31398203

RESUMO

BACKGROUND: Ghana started its national programme to eliminate lymphatic filariasis (LF) in 2000, with mass drug administration (MDA) with ivermectin and albendazole as main strategy. We review the progress towards elimination that was made by 2016 for all endemic districts of Ghana and analyze microfilaria (mf) prevalence from sentinel and spot-check sites in endemic districts. METHODS: We reviewed district level data on the history of MDA and outcomes of transmission assessment surveys (TAS). We further collated and analyzed mf prevalence data from sentinel and spot-check sites. RESULTS: MDA was initiated in 2001-2006 in all 98 endemic districts; by the end of 2016, 81 had stopped MDA after passing TAS and after an average of 11 rounds of treatment (range 8-14 rounds). The median reported coverage for the communities was 77-80%. Mf prevalence survey data were available for 430 communities from 78/98 endemic districts. Baseline mf prevalence data were available for 53 communities, with an average mf prevalence of 8.7% (0-45.7%). Repeated measurements were available for 78 communities, showing a steep decrease in mean mf prevalence in the first few years of MDA, followed by a gradual further decline. In the 2013 and 2014 surveys, 7 and 10 communities respectively were identified with mf prevalence still above 1% (maximum 5.6%). Fifteen of the communities above threshold are all within districts where MDA was still ongoing by 2016. CONCLUSIONS: The MDA programme of the Ghana Health Services has reduced mf prevalence in sentinel sites below the 1% threshold in 81/98 endemic districts in Ghana, yet 15 communities within 13 districts (MDA ongoing by 2016) had higher prevalence than this threshold during the surveys in 2013 and 2014. These districts may need to intensify interventions to achieve the WHO 2020 target.


Assuntos
Erradicação de Doenças/métodos , Filariose Linfática/tratamento farmacológico , Filariose Linfática/epidemiologia , Albendazol/uso terapêutico , Animais , Criança , Pré-Escolar , Filariose Linfática/diagnóstico , Filariose Linfática/prevenção & controle , Doenças Endêmicas , Feminino , Gana/epidemiologia , Pesquisa sobre Serviços de Saúde , Humanos , Ivermectina/uso terapêutico , Masculino , Administração Massiva de Medicamentos/métodos , Microfilárias/patogenicidade , Prevalência , Inquéritos e Questionários , Organização Mundial da Saúde
3.
Clin Infect Dis ; 62(11): 1338-1347, 2016 06 01.
Artigo em Inglês | MEDLINE | ID: mdl-27001801

RESUMO

BACKGROUND: Several African countries have adopted a biannual ivermectin distribution strategy in some foci to control and eliminate onchocerciasis. In 2010, the Ghana Health Service started biannual distribution to combat transmission hotspots and suboptimal responses to treatment. We assessed the epidemiological impact of the first 3 years of this strategy and quantified responses to ivermectin over 2 consecutive rounds of treatment in 10 sentinel communities. METHODS: We evaluated Onchocerca volvulus community microfilarial intensity and prevalence in persons aged ≥20 years before the first, second, and fifth (or sixth) biannual treatment rounds using skin snip data from 956 participants. We used longitudinal regression modeling to estimate rates of microfilarial repopulation of the skin in a cohort of 217 participants who were followed up over the first 2 rounds of biannual treatment. RESULTS: Biannual treatment has had a positive impact, with substantial reductions in infection intensity after 4 or 5 rounds in most communities. We identified 3 communities-all having been previously recognized as responding suboptimally to ivermectin-with statistically significantly high microfilarial repopulation rates. We did not find any clear association between microfilarial repopulation rate and the number of years of prior intervention, coverage, or the community level of infection. CONCLUSIONS: The strategy of biannual ivermectin treatment in Ghana has reduced O. volvulus microfilarial intensity and prevalence, but suboptimal responses to treatment remain evident in a number of previously and consistently implicated communities. Whether increasing the frequency of treatment will be sufficient to meet the World Health Organization's 2020 elimination goals remains uncertain.


Assuntos
Antiparasitários/administração & dosagem , Antiparasitários/uso terapêutico , Ivermectina/administração & dosagem , Ivermectina/uso terapêutico , Oncocercose Ocular , Adulto , Estudos de Coortes , Gana/epidemiologia , Humanos , Masculino , Oncocercose Ocular/tratamento farmacológico , Oncocercose Ocular/epidemiologia , Oncocercose Ocular/parasitologia , Carga Parasitária , Prevalência , Pele/parasitologia , Resultado do Tratamento , Adulto Jovem
4.
Antimicrob Agents Chemother ; 60(6): 3283-90, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-26953191

RESUMO

Trypanosoma brucei parasites are kinetoplastid protozoa that devastate the health and economic well-being of millions of people in Africa through the disease human African trypanosomiasis (HAT). New chemotherapy has been eagerly awaited due to severe side effects and the drug resistance issues plaguing current drugs. Recently, there has been an emphasis on the use of medicinal plants worldwide. Morinda lucida Benth. is a popular medicinal plant widely distributed in Africa, and several research groups have reported on the antiprotozoal activities of this plant. In this study, we identified three novel tetracyclic iridoids, molucidin, ML-2-3, and ML-F52, from the CHCl3 fraction of M. lucida leaves, which possess activity against the GUTat 3.1 strain of T. brucei brucei The 50% inhibitory concentrations (IC50) of molucidin, ML-2-3, and ML-F52 were 1.27 µM, 3.75 µM, and 0.43 µM, respectively. ML-2-3 and ML-F52 suppressed the expression of paraflagellum rod protein subunit 2, PFR-2, and caused cell cycle alteration, which preceded apoptosis induction in the bloodstream form of Trypanosoma parasites. Novel tetracyclic iridoids may be promising lead compounds for the development of new chemotherapies for African trypanosomal infections in humans and animals.


Assuntos
Antiprotozoários/farmacologia , Iridoides/farmacologia , Morinda/química , Plantas Medicinais/química , Tripanossomicidas/farmacologia , Animais , Antiprotozoários/química , Apoptose/efeitos dos fármacos , Ciclo Celular/efeitos dos fármacos , Humanos , Concentração Inibidora 50 , Iridoides/química , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Tripanossomicidas/química , Trypanosoma/efeitos dos fármacos , Trypanosoma/patogenicidade , Tripanossomíase Africana/fisiopatologia
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